2-[(2,4-Dichloro-phenyl)-propylsulfanyl-methyl]-1-methyl-1H-benzoimidazole

Base Information

Chemical Name:2-[(2,4-Dichloro-phenyl)-propylsulfanyl-methyl]-1-methyl-1H-benzoimidazole
CAS No.:96327-86-5
Molecular Formula:C₁₈H₁₈Cl₂N₂S
Molecular Weight:365.326
Hs Code.:

Synonyms:2-[(2,4-Dichloro-phenyl)-propylsulfanyl-methyl]-1-methyl-1H-benzoimidazole

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-[(2,4-Dichloro-phenyl)-propylsulfanyl-methyl]-1-methyl-1H-benzoimidazole

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Technology Process of 2-[(2,4-Dichloro-phenyl)-propylsulfanyl-methyl]-1-methyl-1H-benzoimidazole

There total 3 articles about 2-[(2,4-Dichloro-phenyl)-propylsulfanyl-methyl]-1-methyl-1H-benzoimidazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 18.0%

: 7651-98-1
O-ethyl-S-propyl phosphorochloridate

: 96327-85-4
(2,4-Dichloro-phenyl)-(1-methyl-1H-benzoimidazol-2-yl)-methanol

: 96327-86-5
2-[(2,4-Dichloro-phenyl)-propylsulfanyl-methyl]-1-methyl-1H-benzoimidazole

Guidance literature:: With triethylamine; In dichloromethane; at 25 ℃;
DOI:10.1021/jo00212a017

Reference yield:

: 1632-83-3
1-Methylbenzimidazole

: 96327-86-5
2-[(2,4-Dichloro-phenyl)-propylsulfanyl-methyl]-1-methyl-1H-benzoimidazole

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) n-butyllithium / 1.) Et₂O, -78 deg C, 0.5 h; 2.) 25 deg C, overnight

2: 18 percent / triethylamine / CH₂Cl₂ / 25 °C

With n-butyllithium; triethylamine; In dichloromethane;
DOI:10.1021/jo00212a017

Reference yield:

: 874-42-0
2,4-dichlorobenzaldeyhde

: 96327-86-5
2-[(2,4-Dichloro-phenyl)-propylsulfanyl-methyl]-1-methyl-1H-benzoimidazole

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) n-butyllithium / 1.) Et₂O, -78 deg C, 0.5 h; 2.) 25 deg C, overnight

2: 18 percent / triethylamine / CH₂Cl₂ / 25 °C

With n-butyllithium; triethylamine; In dichloromethane;
DOI:10.1021/jo00212a017